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Browsing publications by Dr Angela Pyle

Newcastle AuthorsTitleYearFull text
Dr Angela Pyle
Dr Fiona Robertson
Professor Robert Taylor
Professor Bobby McFarland
Clinical and Genetic Spectrum of Patients With Mitochondrial Disease in a Pediatric Egyptian Cohort: Novel Variants and Phenotypic Expansion2025
Lucie Taylor
Dr Langping He
Sila Hopton
Dr Angela Pyle
Professor Robert Taylor
COA5 has an essential role in the early stage of mitochondrial complex IV assembly2025
Dr Louise Hyslop
Dr Magomet Aushev
Jordan Marley
Dr Yuko Takeda
Dr Angela Pyle
et al.		Mitochondrial Donation and Preimplantation Genetic Testing for mtDNA Disease2025
Ben Whittle
Dr Hannah Lowes
Dr Dasha Deen
Dr Angela Pyle
Dr Jonathan Coxhead
et al.		Early-stage idiopathic Parkinson's disease is associated with reduced circular RNA expression2024
Alex Bury
Dr Angela Pyle
Dr Amy Vincent
Professor Gavin Hudson
Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues2024
Yasmin Tang
Dr Angela Pyle
Dr Monika Olahova
Professor Robert Taylor
Pathogenic PDE12 variants impair mitochondrial RNA processing causing neonatal mitochondrial disease2024
Dan Hipps
Dr Angela Pyle
Dr Anna Porter
Philip Dobson
Dr Helen Tuppen
et al.		Variant load of mitochondrial DNA in single human mesenchymal stem cells2024
Dr Angela Pyle
Dr Brendan Payne
Dr Jonathan Coxhead
Professor Gavin Hudson
Moira Crosier
et al.		Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos (Nature Cell Biology, (2018), 20, 2, (144-151), 10.1038/s41556-017-0017-8)2023
Dr Yuko Takeda
Dr Louise Hyslop
Dr Meenakshi Choudhary
Dr Fiona Robertson
Dr Angela Pyle
et al.		Feasibility and impact of haplogroup matching for mitochondrial replacement treatment.2023
Dr Dasha Deen
Dr Charlotte Alston
Professor Gavin Hudson
Professor Robert Taylor
Dr Angela Pyle
Genomic Strategies in Mitochondrial Diagnostics2023
Ahmad Alahmad
Dr Angela Pyle
Professor Bobby McFarland
Professor Robert Taylor
Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement2022
Dr Angela Pyle
Professor Robert Taylor
Defining mitochondrial protein functions through deep multiomic profiling2022
Dr Angela Pyle
Dr Helen Griffin
Dr Jonathan Coxhead
Raf Hussain
Professor Gavin Hudson
et al.		Heteroplasmic mitochondrial DNA variants in cardiovascular diseases2022
Dr Sarah Pickett
Dr Dasha Deen
Dr Angela Pyle
Dr Mauro Santibanez Koref
Professor Gavin Hudson
Interactions between nuclear and mitochondrial SNPs and Parkinson's disease risk2022
Dr Katja Menger
Dr James Chapman
Mushtaq Khazeem
Dr Dasha Deen
John Casement
et al.		Two type I topoisomerases maintain DNA topology in human mitochondria2022
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